FDA 510(k) Applications Submitted by Radmedix LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K200726 | 03/20/2020 | AcuityPDR | Radmedix LLC |
| K210919 | 03/29/2021 | AcuityDRe | Radmedix LLC |
| K201058 | 04/21/2020 | Accuvue+ | Radmedix LLC |
| K231709 | 06/12/2023 | AcuityDR 1013 G4, AcuityDR 1417 G4, AcuityDR 1717G4 | Radmedix LLC |
| K193360 | 12/04/2019 | Acuity SDR Standard, Acuity SDR Plus, Acuity FDR Standard | Radmedix LLC |
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